A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346723



Internal ID21004276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:212173661..212178344hg38UCSC Ensembl
chr2:213038386..213043069hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg384684
hg194684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085368
Samples
Known GenesERBB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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